J Korean Neurosurg Soc.  2025 Jan;68(1):7-18. 10.3340/jkns.2024.0100.

Optimizing Glioblastoma, IDH-wildtype Treatment Outcomes : A Radiomics and Support Vector Machine-Based Approach to Overall Survival Estimation

Affiliations
  • 1Department of Neurosurgery, Taipei Medical University Hospital, Taipei, Taiwan
  • 2Department of Computer Science & Engineering, International Institute of Information Technology, Bhubaneswar, India
  • 3Executive Programme in Healthcare Management, Indian Institute of Management, Lucknow, India
  • 4Division of Neurosurgery, Department of Surgery, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan
  • 5Taipei Neuroscience Institute, Taipei Medical University, Taipei, Taiwan

Abstract


Objective
: Glioblastoma multiforme (GBM), particularly the isocitrate dehydrogenase (IDH)-wildtype type, represents a significant clinical challenge due to its aggressive nature and poor prognosis. Despite advancements in medical imaging and its modalities, survival rates have not improved significantly, demanding innovative treatment planning and outcome prediction approaches.
Methods
: This study utilizes a support vector machine (SVM) classifier using radiomics features to predict the overall survival (OS) of GBM, IDH-wildtype patients to short (<12 months) and long (≥12 months) survivors. A dataset comprising multi-parametric magnetic resonance imaging scans from 574 patients was analyzed. Radiomic features were extracted from T1, T2, fluid-attenuated inversion recovery, and T1 with gadolinium (T1GD) sequences. Low variance features were removed, and recursive feature elimination was used to select the most informative features. The SVM model was trained using a k-fold cross-validation approach. Furthermore, clinical parameters such as age, gender, and MGMT (O6-methylguanine-DNA methyltransferase) promoter methylation status were integrated to enhance prediction accuracy.
Results
: The model showed reasonable results in terms of cross-validated area under the curve of 0.84 (95% confidence interval, 0.80–0.90) with (p<0.001) effectively categorizing patients into short and long survivors. Log-rank test (chi-square statistics) analysis for the developed model was 0.00029 along with the 1.20 Cohen’s d effect size. Most importantly, clinical data integration further refined the survival estimates, providing a more fitted prediction that considers individual patient characteristics by Kaplan-Meier curve with p-value <0.0001.
Conclusion
: The proposed method significantly enhances the predictive accuracy of OS outcomes in GBM, IDH-wildtype patients. By integrating detailed imaging features with key clinical indicators, this model offers a robust tool for personalized treatment planning, potentially improving OS.

Keyword

Glioblastoma multiforme; Isocitrate dehydrogenase-wildtype; Overall survival; Radiomics & radiogenomics

Figure

  • Fig. 1. Different structural modalities of multi-parametric magnetic resonance imaging. T1 : T1-weighted, T2 : T2-weighted, FLAIR : fluid-attenuated inversion recovery, T1GD : T1 with gadolinium, Segmask : segmentation mask.

  • Fig. 2. A whole tumor with its subregions such as tumor core (TC) marked as 1, edema (ED) marked as 2, and enhancing tumor (ET) marked as 4 [29].

  • Fig. 3. Survival days on replication cohort.

  • Fig. 4. Overview of the support vector machine (SVM)-based radiomics workflow for predicting survival outcomes in glioblastoma, IDH-wildtype patients. T1 : T1-weighted, T2 : T2-weighted, FLAIR : fluid-attenuated inversion recovery, T1-CE : T1 contrast enhanced, MRI : magnetic resonance imaging, LVR : low variance removal, RFE : recursive feature elimination, MGMT : O6-methylguanine-DNA methyltransferase, KM : Kaplan-Meier, IDH : isocitrate dehydrogenase.

  • Fig. 5. Receiver operating characteristic (ROC) curve across 10-folds. OS : overall survival, AUC : area under the curve.

  • Fig. 6. Survival index on replication cohort.

  • Fig. 7. Survival analysis using Kaplan-Meier curve.


Reference

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